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Issue Date	Title	Author(s)
2012	The dopamine transporter haplotype and reward-related striatal responses in adult ADHD	Hoogman, M.; Onnink, A; Cools, R.; Aarts, E.; Kan, C.C.; Arias Vasquez, A.; Buitelaar, J.K.; Franke, B.
2012	CNTNAP2 and language processing in healthy individuals as measured with ERPs	Kos, M.; Brink, D. van den; Snijders, T.M.; Rijpkema, M.J.P.; Franke, B.; Fernandez, G.S.E.; Hagoort, Peter
2012	CNTNAP2 and Language Processing in Healthy Individuals as Measured with ERPs	Kos, M.; Brink, D. van den; Snijders, T.M.; Rijpkema, M.J.P.; Franke, B.; Fernandez, G.S.E.; Hagoort, P.
2012	Reduced Dopamine Receptor Sensitivity as an Intermediate Phenotype in Alcohol Dependence and the Role of the COMT Val158Met and DRD2 Taq1A Genotypes	Schellekens, A.F.A.; Franke, B.; Ellenbroek, B.A.; Cools, A.R.; Jong, C.A.J. de; Buitelaar, J.K.; Verkes, R.J.
2011	Motorische problemen bij kinderen met ADHD.	Fliers, E.A.; Franke, B.; Buitelaar, J.K.
2011	Assembly of a protein "brush" by end-grafting titin fragments to liposomes	Chami, M.; Franke, B.; Mayans, O.; Kreplak, L.
2011	The interaction between cerebrovascular disease and neuroticism in late-life depression: a cross-sectional study	Wouts, L.; Janzing, J.G.E.; Lampe, I.K.; Franke, B.; Vegt, F. de; Tendolkar, I.; Iersel, M.B. van; Buitelaar, J.K.; Oude Voshaar, R.C.
2011	Human cognitive flexibility depends on dopamine D2 receptor signaling	Holstein, M.G.A. van; Aarts, E.; Schaaf, M.E. van der; Geurts, D.E.M.; Verkes, R.J.; Franke, B.; Schouwenburg, M.R. van; Cools, R.
2011	De invloed van het DRD4 VNTR polymorfisme op adaptatie aan andermans alcoholconsumptie [The DRD4 VNTR polymorphism affects social adaptation of alcohol use: Investigation of a gene-environment interaction]	Larsen, H.; Zwaluw, C.S. van der; Overbeek, G.J.; Granic, I.; Franke, B.; Engels, R.C.M.E.
2011	Integrated genome-wide association study findings: identification of a neurodevelopmental network for attention deficit hyperactivity disorder	Poelmans, G.J.V.; Pauls, D.L.; Buitelaar, J.K.; Franke, B.
2011	A theoretical molecular network for dyslexia: integrating available genetic findings	Poelmans, G.J.V.; Buitelaar, J.K.; Pauls, D.L.; Franke, B.
2011	A review on cognitive and brain endophenotypes that may be common in autism spectrum disorder and attention-deficit/hyperactivity disorder and facilitate the search for pleiotropic genes	Lambregts-Rommelse, N.N.J.; Geurts, H.M.; Franke, B.; Buitelaar, J.K.; Hartman, C.A.
2011	CR1 genotype is associated with entorhinal cortex volume in young healthy adults	Bralten, J.B.; Franke, B.; Arias Vasquez, A.; Heister, A.; Brunner, H.G.; Fernandez, G.S.E.; Rijpkema, M.J.P.
2011	Depressive symptom clusters are differentially associated with atherosclerotic disease	Bus, B.A.A.; Marijnissen, R.M.; Holewijn, S.; Franke, B.; Purandare, N.; Graaf, J. de; Heijer, M. den; Buitelaar, J.K.; Oude Voshaar, R.C.
2011	Depressive symptom clusters are differentially associated with general and visceral obesity	Marijnissen, R.M.; Bus, B.A.A.; Holewijn, S.; Franke, B.; Purandare, N.; Graaf, J. de; Heijer, M. den; Buitelaar, J.K.; Oude Voshaar, R.C.
2011	A functional variant of the serotonin transporter gene (SLC6A4) moderates impulsive choice in attention-deficit/hyperactivity disorder boys and siblings	Sonuga-Barke, E.S.J.; Kumsta, R.; Schlotz, W.; Lasky-Su, J.; Marco, R.; Miranda, A.; Mulas, F.; Oades, R.D.; Banaschewski, T.; Mueller, U.; Andreou, P.; Christiansen, H.; Gabriels, I.; Uebel, H.; Kuntsi, J.; Franke, B.; Buitelaar, J.K.; Ebstein, R.; Gill, M.; Anney, R.; Roeyers, H.; Rothenberger, A.; Sergeant, J.A.; Steinhausen, H.C.; Asherson, P.; Faraone, S.V.
2011	Lowering missing item values in quality-of-life questionnaires: an interventional study	Muller-Buhl, U.; Franke, B.; Hermann, K.; Engeser, P.
2011	Nitric oxide synthase genotype modulation of impulsivity and ventral striatal activity in adult ADHD patients and healthy comparison subjects	Hoogman, M.; Aarts, E.; Zwiers, M.P.; Slaats-Willemse, D.I.E.; Naber, M.; Onnink, M.; Cools, R.; Kan, C.C.; Buitelaar, J.K.; Franke, B.
2011	Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption	Sulem, P.; Gudbjartsson, D.F.; Geller, F.; Prokopenko, I.; Feenstra, B.; Aben, K.K.H.; Franke, B.; Heijer, M. den; Kovacs, P.; Stumvoll, M.; Magi, R.; Yanek, L.R.; Becker, L.C.; Boyd, H.A.; Stacey, S.N.; Walters, G.B.; Jonasdottir, A.; Thorleifsson, G.; Holm, H.; Gudjonsson, S.A.; Rafnar, T.; Bjornsdottir, G.; Becker, D.M.; Melbye, M.; Kong, A.; Tonjes, A.; Thorgeirsson, T.; Thorsteinsdottir, U.; Kiemeney, L.A.L.M.; Stefansson, K.
2011	CDH13 is associated with working memory performance in attention deficit/hyperactivity disorder	Arias Vasquez, A.; Altink, M.E.; Lambregts-Rommelse, N.N.J.; Slaats-Willemse, D.I.E.; Buschgens, C.J.M.; Fliers, E.A.; Faraone, S.V.; Sergeant, J.A.; Oosterlaan, J.; Franke, B.; Buitelaar, J.K.
2011	Genetic variation of the alpha2b-adrenoceptor affects neural correlates of successful emotional memory formation	Urner, M.; Wingen, G.A. van; Franke, B.; Rijpkema, M.J.P.; Fernandez, G.S.E.; Tendolkar, I.
2011	Association of the Alzheimer's gene SORL1 with hippocampal volume in young, healthy adults	Bralten, J.B.; Arias Vasquez, A.; Makkinje, R.R.; Veltman, J.A.; Brunner, H.G.; Fernandez, G.S.E.; Rijpkema, M.J.P.; Franke, B.
2011	Circulating adenosine increases during human experimental endotoxemia but blockade of its receptor does not influence the immune response and subsequent organ injury	Ramakers, B.P.C.; Riksen, N.P.; Broek, P.H.H. van den; Franke, B.; Peters, W.H.M.; Hoeven, J.G. van der; Smits, P.; Pickkers, P.
2011	Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.	Elia, J.; Glessner, J.T.; Wang, K.; Takahashi, N.; Shtir, C.J.; Hadley, D.; Sleiman, P.M.; Zhang, H.; Kim, C.E.; Robison, R.; Lyon, G.J.; Flory, J.H.; Bradfield, J.P.; Imielinski, M.; Hou, C.; Frackelton, E.C.; Chiavacci, R.M.; Sakurai, T.; Rabin, C.; Middleton, F.A.; Thomas, K.A.; Garris, M.; Mentch, F.; Freitag, C.M.; Steinhausen, H.C.; Todorov, A.A.; Reif, A.; Rothenberger, A.; Franke, B.; Mick, E.O.; Roeyers, H.; Buitelaar, J.K.; Lesch, K.P.; Banaschewski, T.; Ebstein, R.P.; Mulas, F.; Oades, R.D.; Sergeant, J.A.; Sonuga-Barke, E.S.J.; Renner, T.J.; Romanos, M.; Romanos, J.; Warnke, A.; Walitza, S.; Meyer, J.; Palmason, H.; Seitz, C.; Loo, S.K.; Smalley, S.L.; Biederman, J.; Kent, L.; Asherson, P.; Anney, R.J.; Gaynor, J.W.; Shaw, P.; Devoto, M.; White, P.S.; Grant, S.F.; Buxbaum, J.D.; Rapoport, J.L.; Williams, N.M.; Nelson, S.F.; Faraone, S.V.; Hakonarson, H.
2011	Genome-wide association study in German patients with attention deficit/hyperactivity disorder	Hinney, A.; Scherag, A.; Jarick, I.; Albayrak, O.; Putter, C. de; Pechlivanis, S.; Dauvermann, M.R.; Beck, S.; Weber, H.; Scherag, S.; Nguyen, T.T.; Volckmar, A.L.; Knoll, N.; Faraone, S.V.; Neale, B.M.; Franke, B.; Cichon, S.; Hoffmann, P.; Nothen, M.M.; Schreiber, S.; Jockel, K.H.; Wichmann, H.E.; Freitag, C.; Lempp, T.; Meyer, J.; Gilsbach, S.; Herpertz-Dahlmann, B.; Sinzig, J.; Lehmkuhl, G.; Renner, T.J.; Warnke, A.; Romanos, M.; Lesch, K.P.; Reif, A.; Schimmelmann, B.G.; Hebebrand, J.
2011	Copy number variations of chromosome 16p13.1 region associated with schizophrenia	Ingason, A.; Rujescu, D.; Cichon, S.; Sigurdsson, E.; Sigmundsson, T.; Pietilainen, O.P.H.; Buizer-Voskamp, J.E.; Strengman, E.; Francks, C.; Muglia, P.; Gylfason, A.; Gustafsson, O.; Olason, P.I.; Steinberg, S.; Hansen, T.; Jakobsen, K.D.; Rasmussen, H.B.; Giegling, I.; Moller, H.J.; Hartmann, A.; Crombie, C.; Fraser, G.; Walker, N.; Lonnqvist, J.; Suvisaari, J.; Tuulio-Henriksson, A.; Bramon, E.; Kiemeney, L.A.L.M.; Franke, B.; Murray, R.; Vassos, E.; Toulopoulou, T.; Muhleisen, T.W.; Tosato, S.; Ruggeri, M.; Djurovic, S.; Andreassen, O.A.; Zhang, Z.; Werge, T.; Ophoff, R.A.; Rietschel, M.; Nothen, M.M.; Petursson, H.; Stefansson, H.; Peltonen, L.; Collier, D.; Stefansson, K.; St Clair, D.M.
2011	Maternally derived microduplications at 15q11-q13: implication of imprinted genes in psychotic illness	Ingason, A.; Kirov, G.; Giegling, I.; Hansen, T.; Isles, A.R.; Jakobsen, K.D.; Kristinsson, K.T.; Roux, L. le; Gustafsson, O.; Craddock, N.; Moller, H.J.; McQuillin, A.; Muglia, P.; Cichon, S.; Rietschel, M.; Ophoff, R.A.; Djurovic, S.; Andreassen, O.A.; Pietilainen, O.P.H.; Peltonen, L.; Dempster, E.; Collier, D.A.; St Clair, D.; Rasmussen, H.B.; Glenthoj, B.Y.; Kiemeney, L.A.L.M.; Franke, B.; Tosato, S.; Bonetto, C.; Saemundsen, E.; Hreidarsson, S.J.; Nothen, M.M.; Gurling, H.; O'Donovan, M.C.; Owen, M.J.; Sigurdsson, E.; Petursson, H.; Stefansson, H.; Rujescu, D.; Stefansson, K.; Werge, T.
2011	Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: a meta-analysis in four European populations	Sanchez-Mora, C.; Ribases, M.; Casas, M.; Bayes, M.; Bosch, R.; Fernandez-Castillo, N.; Brunso, L.; Jacobsen, K.K.; Landaas, E.T.; Lundervold, A.J.; Gross-Lesch, S.; Kreiker, S.; Jacob, C.P.; Lesch, K.P.; Buitelaar, J.K.; Hoogman, M.; Kiemeney, L.A.L.M.; Kooij, J.J.; Mick, E.; Asherson, P.; Faraone, S.V.; Franke, B.; Reif, A.; Johansson, S.; Haavik, J.; Ramos-Quiroga, J.A.; Cormand, B.
2011	DIRAS2 is associated with adult ADHD, related traits, and co-morbid disorders	Reif, A.; Nguyen, T.T.; Weissflog, L.; Jacob, C.P.; Romanos, M.; Renner, T.J.; Buttenschon, H.N.; Kittel-Schneider, S.; Gessner, A.; Weber, H.; Neuner, M.; Gross-Lesch, S.; Zamzow, K.; Kreiker, S.; Walitza, S.; Meyer, J.; Freitag, C.M.; Bosch, R.; Casas, M.; Gomez, N.; Ribases, M.; Bayes, M.; Buitelaar, J.K.; Kiemeney, L.A.L.M.; Kooij, J.J.; Kan, C.C.; Hoogman, M.; Johansson, S.; Jacobsen, K.K.; Knappskog, P.M.; Fasmer, O.B.; Asherson, P.; Warnke, A.; Grabe, H.J.; Mahler, J.; Teumer, A.; Volzke, H.; Mors, O.N.; Schafer, H.; Ramos-Quiroga, J.A.; Cormand, B.; Haavik, J.; Franke, B.; Lesch, K.P.
2011	Common variants in DGKK are strongly associated with risk of hypospadias	Zanden, L.F. van der; Rooij, I.A. van; Feitz, W.F.J.; Knight, J.; Donders, A.R.T.; Renkema, K.Y.; Bongers, M.H.F.; Vermeulen, S.; Kiemeney, L.A.L.M.; Veltman, J.A.; Arias Vasquez, A.; Zhang, X.; Markljung, E.; Qiao, L.; Baskin, L.S.; Nordenskjold, A.; Roeleveld, N.; Franke, B.; Knoers, N.V.A.M.
2011	The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects	Rizzi, T.S.; Arias Vasquez, A.; Rommelse, N.N.; Kuntsi, J.; Anney, R.; Asherson, P.; Buitelaar, J.K.; Banaschewski, T.; Ebstein, R.; Ruano, D.; Sluis, S. Van der; Markunas, C.A.; Garrett, M.E.; Ashley-Koch, A.E.; Kollins, S.H.; Anastopoulos, A.D.; Hansell, N.K.; Wright, M.J.; Montgomery, G.W.; Martin, N.G.; Harris, S.E.; Davies, G.; Tenesa, A.; Porteous, D.J.; Starr, J.M.; Deary, I.J.; St Pourcain, B.; Davey Smith, G.; Timpson, N.J.; Evans, D.M.; Gill, M.; Miranda, A.; Mulas, F.; Oades, R.D.; Roeyers, H.; Rothenberger, A.; Sergeant, J.A.; Sonuga-Barke, E.S.J.; Steinhausen, H.C.; Taylor, E.; Faraone, S.V.; Franke, B.; Posthuma, D.
2011	The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples	Rodriguez-Rodriguez, L.; Taib, W.R.; Topless, R.; Steer, S.; Gonzalez-Escribano, M.F.; Balsa, A.; Pascual-Salcedo, D.; Gonzalez-Gay, M.A.; Raya, E.; Fernandez-Gutierrez, B.; Gonzalez-Alvaro, I.; Bottini, N.; Witte, T.J.M. de; Viken, M.K.; Coenen, M.J.H.; Riel, P.L. van; Franke, B.; Heijer, M. den; Radstake, T.R.D.J.; Wordsworth, P.; Lie, B.A.; Merriman, T.R.; Martin, J.
2010	The brain-derived neurotrophic factor Val66Met polymorphism affects memory formation and retrieval of biologically salient stimuli	Wingen, G.A. van; Rijpkema, M.J.P.; Franke, B.; Eijndhoven, P. van; Tendolkar, I.; Verkes, R.J.; Buitelaar, J.K.; Fernández, G.
2010	Genetic variation in CACNA1C, a gene associated with bipolar disorder, influences brainstem rather than gray matter volume in healthy individuals	Franke, B.; Arias Vasquez, A.; Veltman, J.A.; Brunner, H.G.; Rijpkema, M.J.P.; Fernández, G.
2010	Acute stress modulates genotype effects on amygdala processing in humans	Cousijn, H.; Rijpkema, M.J.P.; Qin, S.; Marle, H.J.F. van; Franke, B.; Hermans, E.J.; Wingen, G. van; Fernández, G.
2010	Striatal dopamine mediates the interface between motivational and cognitive control in humans: Evidence from genetic imaging	Aarts, E.; Roelofs, A.; Franke, B.; Rijpkema, Mark; Fernández, G.; Helmich, R.C.G.; Cools, R.
2010	Striatal dopamine mediates the interface between motivational and cognitive control in humans : evidence from genetic imaging	Aarts, E.; Roelofs, A.; Franke, B.; Rijpkema, Mark; Fernández, G.; Helmich, R.C.G.
2010	Striatal dopamine mediates the interface between motivational and cognitive control in humans : evidence from genetic imaging	Aarts, E.; Roelofs, A.; Franke, B.; Rijpkema, M.J.P.; Fernandez, G.S.E.; Helmich, R.C.G.; Cools, R.
2010	Do candidate genes discriminate patients with an autism spectrum disorder from those with attention deficit/hyperactivity disorder and is there an effect of lifetime substance use disorders?	Sizoo, B.B.; Brink, W. van den; Franke, B.; Vasquez, A.A.; Wijngaarden-Cremers, P. van; Gaag, R.J. van der
2010	Molecular genetics of attention-deficit/hyperactivity disorder: an overview.	Banaschewski, T.; Becker, K.; Scherag, S.; Franke, B.; Coghill, D.
2010	Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.	Rommelse, N.N.J.; Franke, B.; Geurts, H.M.; Hartman, C.A.; Buitelaar, J.K.
2010	ADHD and DAT1: further evidence of paternal over-transmission of risk alleles and haplotype.	Hawi, Z.; Kent, L.; Hill, M.; Anney, R.J.; Brookes, K.J.; Barry, E.; Franke, B.; Banaschewski, T.; Buitelaar, J.K.; Ebstein, R.; Miranda, A.; Oades, R.D.; Roeyers, H.; Rothenberger, A.; Sergeant, J.A.; Sonuga-Barke, E.; Steinhausen, H.C.; Faraone, S.V.; Asherson, P.; Gill, M.
2010	A Variable-Number-of-Tandem-Repeats Polymorphism in the Dopamine D4 Receptor Gene Affects Social Adaptation of Alcohol Use. Investigation of a Gene-Environment Interaction	Larsen, H.; Zwaluw, C.S. van der; Overbeek, G.J.; Granic, I.; Franke, B.; Engels, R.C.M.E.
2010	Interaction between dopamine D2 receptor genotype and parental rule-setting in adolescent alcohol use: evidence for a gene-parenting interaction.	Zwaluw, C.S. van der; Engels, R.C.; Vermulst, A.A.; Franke, B.; Buitelaar, J.K.; Verkes, R.J.; Scholte, R.H.
2010	A variable-number-of-tandem-repeats polymorphism in the dopamine D4 receptor gene affects social adaptation of alcohol use: investigation of a gene-environment interaction.	Larsen, H.; Zwaluw, C.S. van der; Overbeek, G.; Granic, I.; Franke, B.; Engels, R.C.
2010	Striatal dopamine mediates the interface between motivational and cognitive control in humans: Evidence from genetic imaging	Aarts, E.; Roelofs, A.P.A.; Franke, B.; Rijpkema, M.J.P.; Fernandez, G.S.E.; Helmich, R.C.G.; Cools, R.
2010	Acute stress modulates genotype effects on amygdala processing in humans.	Cousijn, H.; Rijpkema, M.J.P.; Qin, S.; Marle, H.J.F. van; Franke, B.; Hermans, E.J.; Wingen, G.A. van; Fernandez, G.S.E.
2010	Case-control genome-wide association study of attention-deficit/hyperactivity disorder.	Neale, B.M.; Medland, S.; Ripke, S.; Anney, R.J.; Asherson, P.; Buitelaar, J.K.; Franke, B.; Gill, M.; Kent, L.; Holmans, P.; Middleton, F.; Thapar, A.; Lesch, K.P.; Faraone, S.V.; Daly, M.; Nguyen, T.T.; Schafer, H.; Steinhausen, H.C.; Reif, A.; Renner, T.J.; Romanos, M.; Romanos, J.; Warnke, A.; Walitza, S.; Freitag, C.; Meyer, J.; Palmason, H.; Rothenberger, A.; Hawi, Z.; Sergeant, J.A.; Roeyers, H.; Mick, E.; Biederman, J.
2010	Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations.	Johansson, S.; Halmoy, A.; Mavroconstanti, T.; Jacobsen, K.K.; Landaas, E.T.; Reif, A.; Jacob, C.; Boreatti-Hummer, A.; Kreiker, S.; Lesch, K.P.; Kan, C.C.; Kooij, J.J.; Kiemeney, L.A.L.M.; Buitelaar, J.K.; Franke, B.; Ribases, M.; Bosch, R.; Bayes, M.; Casas, M.; Ramos-Quiroga, J.A.; Cormand, B.; Knappskog, P.; Haavik, J.
2010	Actual motor performance and self-perceived motor competence in children with attention-deficit hyperactivity disorder compared with healthy siblings and peers.	Fliers, E.A.; Hoog, M.L.A. de; Franke, B.; Faraone, S.V.; Lambregts-Rommelse, N.N.J.; Buitelaar, J.K.; Nijhuis-Van der Sanden, M.W.G.

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